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季铵盐在高岭石表面的吸附特性 被引量:5

Absorption characteristics of quaternary ammonium on kaolinite
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摘要 采用吸附等温线测量、荧光探针技术以及沉降实验研究季铵盐在高岭石表面的吸附特性。采用溴百里酚蓝标记分光光度法测量吸附等温线,利用芘荧光探针技术从微观上描述吸附特性和吸附层结构。结果表明:在低浓度范围内(0~1 mmol/L),通过离子交换和静电作用共吸附致吸附量达到完全吸附;随着浓度增加,季铵盐的吸附量与平衡浓度呈直线关系,静电吸附为主;当浓度增大到一定范围内,吸附量增加缓慢,主要以季铵盐分子间疏水缔合作用产生吸附;当浓度达到CMC时,吸附达到平衡。十六烷基三甲基氯化铵(CTAC)和十二烷基三甲基氯化铵(DTAC)的饱和吸附量分别为5.3μmol/m2和5.0μmol/m2,而DTAC临界胶束浓度CMC(13 mmol/L)比CTAC(8mmol/L)的大,当CTAC和DTAC浓度为CMC时,沉降产率达到最大,分别为97.84%和95.39%。 The adsorption characteristics of quaternary ammonium salt on kaolinite were studied using adsorption isotherm, fluorescence probe test and sedimentation test. The adsorption isotherm was measured using spectrophotometric marked by bromothymol blue method. The adsorption layer structure model and adsorption characteristics of quaternary ammonium salts on kaolinite were explained further from microscopic level using pyrene fluorescent probe technology. The results indicate that the cationic surfactant is completely absorbed due to electrostatic interactions and ion exchange on kaolinite surfaces in the low concentration range (0-1 mmol/L). With the increase of surfactant concentration, the relationship between adsorption and equilibrium concentration is linear, mainly due to electrostatic interactions. With a further increase in surfactant concentration, the adsorption increases slowly due to hydrophobic association of chain-chain interactions. Finally, the adsorption runs to saturation. The saturation adsorbed amounts of CTAC and DTAC are 5.3 ~tmol/m/ and 5.0 pmol/m2, respectively. But the critical micelle concentration(CMC) of DTAC(13 mmol/L) is large than that of CTAC(8 mmol/L). When the concentrations of CTAC and DTAC reach CMC, Settling yields are 97.84% and 95.39%, respectively. And the adsorption characteristics were verified from macroscopic level by sedimentation test.
出处 《中南大学学报(自然科学版)》 EI CAS CSCD 北大核心 2013年第11期4379-4384,共6页 Journal of Central South University:Science and Technology
基金 国家自然科学基金资助项目(50974134 51304162)
关键词 高岭石 DTAC CTAC 吸附 芘荧光探针 kaolinite DTAC CTAC adsorption pyrene fluorescence probe
作者简介 通信作者 蒋昊(1971-),女,湖南湘阴人,高级实验师,从事浮选理论研究;电话:13908477086 E—mail:jianghao-1@126.com
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  • 1曹学锋,胡岳华,徐兢.Synthesis of γ-alkoxy-propylamines and their collecting properties on aluminosilicate minerals[J].Journal of Central South University of Technology,2004,11(3):280-285. 被引量:12
  • 2李继山,姚同玉.分光光度法测定阳离子表面活性剂在砂岩表面的吸附[J].日用化学工业,2005,35(3):188-191. 被引量:15
  • 3Williams D J A,Williams K P. Electrophoresis and Zeta Potential of Kaolinite[J]. Journal of Colloid and Interface Science,1978,65 : 79 - 87.
  • 4Brindley G W, Robinson K. The Structure of Kaolinite[J ]. Mineralogical Magazine, 1946,31:781 -786.
  • 5Hyde S T. Hyperbolic and Elliptic Layer Warping in Some Sheet Alumino-silicates[J]. Physics and Chemistry of Minerals,1993,20:190-220.
  • 6Michaelian K H, Yariv S, Nasser A. Study of the Interaction Between Caesium Bromide and Kaolinite by Photoacoustic and Fiffuse Reflectance Infrared Spectroscopy[J]. Canadian Journal of Chemistry, 1991,69: 749- 754.
  • 7Hong H L, Wang Q Y,Chang J P, et al. Occurrence and Distribution of Invisible Gold in the Shewushan Supergene Gold Deposit Southeastern Hubei, China[J]. Canadian Mineralogist, 1999,37(6) : 1525 - 1531.
  • 8Ferris A P,Jepsm W B. The Exchange Capacities of Kaolinite and the Preparation of Homoionic Clays[J]. Journal of Colloid and Interface Science, 1975,51:245-259.
  • 9Haderlein S B,Schwarzenbach R P. Admrption of Substituted Nitrobenzenes and Nitrophenols to Mineral Surfaces[J ]. Environmental Science and Technology, 1993,27 : 316 - 326.
  • 10Wieland E, Stumm W. Dissolution Kinetics of Kaolinite in Acidic Aqueous Solutions at 25℃[J].Geochimica et Cosmochimica Acta, 1992,56 : 3339 - 3355.

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